Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1719406Generated: November 2, 2026

Pentyl nitrite → Amyl Acetate

https://huagongshe.com/reaction/1719406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPentyl nitriteHCID 10026—
ReactantKeteneHCID 10038—
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 178418416HCID 178418416—
CatalystTetrabutylammonium ChlorideHCID 70681—
SolventHeptaneHCID 8900—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductAmyl AcetateHCID 1234814%

Reaction Steps

To the same reaction vessel as in Example 9 were charged bistriphenylphosphinedibromopalladium (0.198 g, 0.25 mmole), stannous chloride (0.095 g, 0.5 mmole), tetra-n-butylammonium chloride (0.139 g, 0.5 mmole) and n-amyl nitrite (55 ml, 368.9 mmoles), together with n-heptane (175 ml) and N-methylpyrrolidone (25 ml). Then, ketene, carbon monooxide and nitrogen were introduced to the mixture at the rate of 11.4 ml/min (0.51 mmole/min), 300 ml/min and 100 ml/min, respectively, and the reaction was effected at 90° C. for 4 hours. During the reaction, 10 ml of a solution of triphenylphosphine (0.061 g, 0.25 mmole) and stannous chloride (0.0475 g, 0.25 mmole) of N-methylpyrrolidone was added to the reaction system in 2.5 ml portions every 1 hour. The gas chromatographic analysis revealed that di-n-amyl malonate (103.9 mmoles, 84.9%) and n-amyl acetate (17.1 mmoles, 14.0%) were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04539423
Source datasetuspto-grants-1985_09
ORD IDord-a860056bd5184781924258318fe60926
Source noteuspto-grants-1985_09